Laurent Villard

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with α-thalassemia (ATR-X syndrome)

Richard J. Gibbons, David J. Picketts, Laurent Villard et al. · Cell · 1995 · 628 citations · Full text

Transcriptional Regulation, Developmental Biology, Mendelian Disorder +8

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Markus Wolff, Katrine M. Johannesen, Ulrike B. S. Hedrich et al. · Brain · 2017 · 558 citations · Full text

Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes

Sabine Endele, Georg Rosenberger, Kirsten Geider et al. · Nature Genetics · 2010 · 502 citations

Developmental Biology, Molecular Neuroscience, Brain Development +13

Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice

Jean‐Charles Viemari, Jean‐Christophe Roux, Andrew K. Tryba et al. · Journal of Neuroscience · 2005 · 281 citations · Full text

Mecp2-/y Mice, Neurodegenerative Diseases, Molecular Physiology +14

Two affected boys in a Rett syndrome family

Laurent Villard, Arlette Kpebe, Carlos Cardoso et al. · Neurology · 2000 · 194 citations